Coronavirus nucleocapsid proteins: a multifaceted modulator in the innate immune evasion

Coronaviruses are capable of inducing diverse infectious diseases that pose significant threats to the public health and the economic development. With a single positive-stranded RNA genome, coronaviruses utilize viral proteins to execute diverse immune escape strategies to facilitate their replication. Of all the identified structural proteins and non-structural proteins within the coronaviruses, nucleocapsid (N) protein is highly conserved and is the most abundant viral protein in infected host cells. N protein regulates the more complex and diverse mechanisms through which viruses suppress host immunity. In this review, we analyzed the basic structure of coronavirus N protein, and further elaborate on its multifaceted regulatory functions in the virion assembly, pathogenesis, host innate immune responses, as well as the innate immunity-related programmed cell death and cell cycle, and also other cell processes. A better understanding of the immune evasion strategy regulated by N protein will help to provide a theoretical basis for the development of broad-spectrum anti-coronavirus drugs targeting N proteins.

Authors

Institutions

Publication Details

Journal
Frontiers in Microbiology
Published
2025-12-09
DOI
https://doi.org/10.3389/fmicb.2025.1658339
Citations
1
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
1.40

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Coronavirus nucleocapsid proteins: a multifaceted modulator in the innate immune evasion

Lei Zhou, Wanqing Lu, Yuting Xiao, Zhigang Song et al.
1 citations
Frontiers in Microbiology
SARS-CoV-2 and COVID-19 Research
1.40
article

Coronavirus nucleocapsid proteins: a multifaceted modulator in the innate immune evasion

Lei Zhou, Wanqing Lu, Yuting Xiao, Zhigang Song, Xiaoliang Li, Weihuan Fang, Jidong Xu
article en
1 citations

Abstract

Coronaviruses are capable of inducing diverse infectious diseases that pose significant threats to the public health and the economic development. With a single positive-stranded RNA genome, coronaviruses utilize viral proteins to execute diverse immune escape strategies to facilitate their replication. Of all the identified structural proteins and non-structural proteins within the coronaviruses, nucleocapsid (N) protein is highly conserved and is the most abundant viral protein in infected host cells. N protein regulates the more complex and diverse mechanisms through which viruses suppress host immunity. In this review, we analyzed the basic structure of coronavirus N protein, and further elaborate on its multifaceted regulatory functions in the virion assembly, pathogenesis, host innate immune responses, as well as the innate immunity-related programmed cell death and cell cycle, and also other cell processes. A better understanding of the immune evasion strategy regulated by N protein will help to provide a theoretical basis for the development of broad-spectrum anti-coronavirus drugs targeting N proteins.

Frontiers in MicrobiologyVol. 16
Zhejiang Academy of Social Sciences (CN), ZheJiang Academy of Agricultural Sciences (CN), Rural Development Institute (CN), Zhejiang Medicine (China) (CN), Zhejiang University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 14%
SARS-CoV-2 and COVID-19 Research
1.40
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Coronavirus nucleocapsid proteins: a multifaceted modulator in the innate immune evasion — Lei Zhou, Wanqing Lu, et al. · Frontiers in Microbiology (2025) | TGRS Research Map | TGRS